NEW! - AMA CPT Advanced Coding Pack

×

Unlock the full potential of your medical coding capabilities with the CPT® Advanced Coding Pack from the American Medical Association (AMA). Designed for professional medical coders, auditors, and billers like you, this comprehensive suite of resources provides everything you need to navigate the complexities of the CPT code set with confidence and precision.

 

Advanced Coding Pack includes:

1. CPT Assistant - Newsletter with official education and guidance
2. CPT Knowledge Base - Commonly asked coding questions answered by the experts
3. CPT Vignettes - Comprehensive clinical examples.

Add to your Find-A-Code subscription for $300 / person

Learn More and Subscribe

close

5C51.2 Disorders of glyoxylate metabolism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Primary hyperoxaluria, or oxalosis, is a rare metabolic disorder transmitted as an autosomal recessive disease, including both type 1, the most frequent, and type 2, extremely rare. Hyperoxaluria type 1 is due to a defect of the peroxysomal hepatic enzyme L-alanine: glyoxylate aminotransferase (AGT). Hyperoxaluria type 2 is extremely rare and is due to glycerate dehydrogenase deficiency.

sections/codes in this section (5C51.2-5C51.2)

• Primary hyperoxaluria type 1  (5C51.20)
• Other specified disorders of glyoxylate metabolism  (5C51.2Y)
• Disorders of glyoxylate metabolism, unspecified  (5C51.2Z)

Thank you for choosing Find-A-Code, please Sign In to remove ads.